Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
T |
A |
14: 70,393,392 (GRCm39) |
H299L |
probably damaging |
Het |
Abcb4 |
C |
T |
5: 8,985,180 (GRCm39) |
A687V |
probably benign |
Het |
Abtb3 |
A |
G |
10: 85,465,130 (GRCm39) |
T657A |
probably damaging |
Het |
Adam20 |
A |
G |
8: 41,248,048 (GRCm39) |
T53A |
probably benign |
Het |
Afg1l |
G |
A |
10: 42,330,490 (GRCm39) |
T59I |
probably benign |
Het |
AI837181 |
A |
G |
19: 5,476,329 (GRCm39) |
Q164R |
probably benign |
Het |
Anapc15 |
T |
A |
7: 101,546,974 (GRCm39) |
I12N |
probably benign |
Het |
Ankrd55 |
A |
C |
13: 112,499,988 (GRCm39) |
E278D |
probably benign |
Het |
Axin2 |
A |
G |
11: 108,833,125 (GRCm39) |
T437A |
probably benign |
Het |
BC051665 |
T |
C |
13: 60,931,895 (GRCm39) |
D168G |
probably damaging |
Het |
Cd200 |
C |
T |
16: 45,212,664 (GRCm39) |
R261H |
probably benign |
Het |
Clk1 |
G |
A |
1: 58,460,261 (GRCm39) |
S123L |
probably benign |
Het |
Csrnp2 |
A |
T |
15: 100,382,571 (GRCm39) |
D156E |
probably damaging |
Het |
Ctss |
C |
T |
3: 95,452,695 (GRCm39) |
Q159* |
probably null |
Het |
Dennd2b |
C |
A |
7: 109,156,043 (GRCm39) |
E236* |
probably null |
Het |
Dip2a |
A |
G |
10: 76,157,327 (GRCm39) |
S93P |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Dync1h1 |
C |
A |
12: 110,624,560 (GRCm39) |
T3700N |
probably damaging |
Het |
Ephb6 |
G |
A |
6: 41,593,743 (GRCm39) |
R542Q |
probably benign |
Het |
Fmo3 |
T |
C |
1: 162,781,880 (GRCm39) |
D491G |
possibly damaging |
Het |
Galnt14 |
A |
T |
17: 73,843,888 (GRCm39) |
M140K |
probably benign |
Het |
Ghsr |
T |
C |
3: 27,425,986 (GRCm39) |
V14A |
probably benign |
Het |
Gm17546 |
C |
A |
15: 95,727,843 (GRCm39) |
|
probably benign |
Het |
Gprc5c |
G |
T |
11: 114,755,093 (GRCm39) |
V257L |
possibly damaging |
Het |
Hc |
A |
G |
2: 34,909,682 (GRCm39) |
V866A |
probably benign |
Het |
Hoxb6 |
G |
A |
11: 96,190,348 (GRCm39) |
G116R |
probably damaging |
Het |
Hykk |
A |
G |
9: 54,827,890 (GRCm39) |
Y43C |
probably damaging |
Het |
Jade2 |
T |
C |
11: 51,711,975 (GRCm39) |
T495A |
probably benign |
Het |
Kansl1 |
A |
T |
11: 104,233,798 (GRCm39) |
V755E |
possibly damaging |
Het |
Lrp2 |
T |
A |
2: 69,309,457 (GRCm39) |
D2814V |
probably damaging |
Het |
Mbd5 |
T |
A |
2: 49,147,009 (GRCm39) |
N406K |
probably damaging |
Het |
Met |
A |
T |
6: 17,491,928 (GRCm39) |
D230V |
probably damaging |
Het |
Mrgprx2 |
A |
T |
7: 48,132,584 (GRCm39) |
V78D |
probably damaging |
Het |
Mrpl20 |
A |
G |
4: 155,892,993 (GRCm39) |
T112A |
possibly damaging |
Het |
Nek11 |
T |
A |
9: 105,040,362 (GRCm39) |
E566D |
probably damaging |
Het |
Nostrin |
T |
C |
2: 69,005,923 (GRCm39) |
S235P |
probably damaging |
Het |
Npas4 |
C |
A |
19: 5,036,805 (GRCm39) |
S453I |
probably benign |
Het |
Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
Psg18 |
A |
T |
7: 18,084,711 (GRCm39) |
Y128* |
probably null |
Het |
Ptges3l |
A |
T |
11: 101,310,010 (GRCm39) |
|
probably benign |
Het |
Pus1 |
T |
C |
5: 110,927,796 (GRCm39) |
|
probably benign |
Het |
Raf1 |
T |
A |
6: 115,621,544 (GRCm39) |
S12C |
possibly damaging |
Het |
Rps6-ps2 |
T |
G |
8: 89,533,206 (GRCm39) |
|
noncoding transcript |
Het |
Slc5a4b |
A |
G |
10: 75,898,073 (GRCm39) |
L547P |
probably damaging |
Het |
Socs3 |
A |
G |
11: 117,858,654 (GRCm39) |
S135P |
probably benign |
Het |
Spata31d1e |
T |
C |
13: 59,890,047 (GRCm39) |
D591G |
probably benign |
Het |
Stra6l |
G |
A |
4: 45,873,682 (GRCm39) |
V281M |
possibly damaging |
Het |
Suco |
G |
A |
1: 161,661,977 (GRCm39) |
T818I |
possibly damaging |
Het |
Syde1 |
A |
T |
10: 78,424,731 (GRCm39) |
V367D |
probably damaging |
Het |
Tet3 |
A |
T |
6: 83,353,865 (GRCm39) |
L932* |
probably null |
Het |
Trpm7 |
G |
A |
2: 126,655,105 (GRCm39) |
L1278F |
possibly damaging |
Het |
Wfdc6b |
A |
G |
2: 164,459,214 (GRCm39) |
Q92R |
possibly damaging |
Het |
|
Other mutations in Vmn1r168 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01761:Vmn1r168
|
APN |
7 |
23,241,070 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02621:Vmn1r168
|
APN |
7 |
23,240,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02650:Vmn1r168
|
APN |
7 |
23,240,916 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4466001:Vmn1r168
|
UTSW |
7 |
23,240,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R0320:Vmn1r168
|
UTSW |
7 |
23,240,767 (GRCm39) |
missense |
probably benign |
0.12 |
R1595:Vmn1r168
|
UTSW |
7 |
23,240,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1618:Vmn1r168
|
UTSW |
7 |
23,240,725 (GRCm39) |
missense |
probably benign |
0.02 |
R1808:Vmn1r168
|
UTSW |
7 |
23,240,184 (GRCm39) |
missense |
probably benign |
0.05 |
R2418:Vmn1r168
|
UTSW |
7 |
23,240,824 (GRCm39) |
missense |
probably benign |
0.05 |
R2419:Vmn1r168
|
UTSW |
7 |
23,240,824 (GRCm39) |
missense |
probably benign |
0.05 |
R4864:Vmn1r168
|
UTSW |
7 |
23,240,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R5269:Vmn1r168
|
UTSW |
7 |
23,240,839 (GRCm39) |
missense |
probably benign |
0.40 |
R6265:Vmn1r168
|
UTSW |
7 |
23,240,961 (GRCm39) |
missense |
probably benign |
|
R6353:Vmn1r168
|
UTSW |
7 |
23,240,944 (GRCm39) |
missense |
probably benign |
0.02 |
R6768:Vmn1r168
|
UTSW |
7 |
23,240,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R6921:Vmn1r168
|
UTSW |
7 |
23,240,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Vmn1r168
|
UTSW |
7 |
23,240,487 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8749:Vmn1r168
|
UTSW |
7 |
23,240,428 (GRCm39) |
missense |
probably benign |
0.10 |
R9749:Vmn1r168
|
UTSW |
7 |
23,240,237 (GRCm39) |
missense |
probably damaging |
0.98 |
R9768:Vmn1r168
|
UTSW |
7 |
23,240,509 (GRCm39) |
missense |
probably benign |
0.02 |
|